5072-45-7 Usage
Uses
Used in Organic Synthesis:
2,6-DIMETHYL-PIPERIDINIUM CHLORIDE is used as a phase-transfer catalyst for facilitating reactions between organic and inorganic compounds, enhancing the efficiency and selectivity of various organic synthesis processes.
Used in Pharmaceutical Production:
2,6-DIMETHYL-PIPERIDINIUM CHLORIDE is used as a reagent and intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and improving the manufacturing processes.
Used in Agrochemicals:
2,6-DIMETHYL-PIPERIDINIUM CHLORIDE is used as a component in the production of agrochemicals, such as pesticides and herbicides, to improve their effectiveness and performance in agricultural applications.
Used in Polymerization Reactions:
2,6-DIMETHYL-PIPERIDINIUM CHLORIDE is used as a catalyst in polymerization reactions, aiding in the formation of polymers with desired properties for various industrial applications.
Used in Surfactant Synthesis:
2,6-DIMETHYL-PIPERIDINIUM CHLORIDE is used as a surfactant in the synthesis of nanoparticles, playing a crucial role in controlling the size, shape, and stability of the nanoparticles for applications in various industries.
Used in Manufacturing of Pharmaceuticals:
2,6-DIMETHYL-PIPERIDINIUM CHLORIDE is used as a key component in the manufacturing process of pharmaceuticals, ensuring the quality and efficacy of the final products.
Check Digit Verification of cas no
The CAS Registry Mumber 5072-45-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,7 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5072-45:
(6*5)+(5*0)+(4*7)+(3*2)+(2*4)+(1*5)=77
77 % 10 = 7
So 5072-45-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H15N.ClH/c1-6-4-3-5-7(2)8-6;/h6-8H,3-5H2,1-2H3;1H/t6-,7+;
5072-45-7Relevant academic research and scientific papers
Diastereoselective synthesis of 2,5-dimethylpyrrolidines and 2,6- dimethylpiperidines by reductive amination of 2,5-hexanedione and 2,6- heptanedione with hydride reagents
Boga,Manescalchi,Savoia
, p. 4709 - 4722 (2007/10/02)
The reductive amination of 2,5-hexanedione and 2,6-heptanedione with ammonia and primary amines in the presence of hydride reagents afforded 2,5- dimethylpyrrolidines and 2,6-dimethylpiperidines with variable diastereoselectivity, as the cis/trans ratio was affected by the size of the ring formed and the steric and electronic properties of the nitrogen substituent. Increasing the bulkiness of the nitrogen substituent, the cis pyrrolidines and the trans-piperidines were obtained with enhanced selectivity.
Synthesis of trans-2,6-Dialkylpiperidines by Intramolecular Amidomercuriation and by 1,3-Cycloaddition of Alkenes to 2-Methyl-2,3,4,5-tetrahydropyridine Oxide
Adams, David R.,Carruthers, William,Williams, Michael J.,Crowley, Patrick J.
, p. 1507 - 1513 (2007/10/02)
Intramolecular amidomercuriation of methyl N-hept-6-en-2-ylcarbamate and reaction of the resulting organomercurial with sodium borohydride in the presence of acrylonitrile or dec-1-en-3-one has been used to prepare trans-2,6-dialkylpiperidines.A more stereoselective route lies in the cycloaddition of alkenes to 2-alkyl-2,3,4,5-tetrahydropyridine oxides followed by reductive cleavage of the resulting perhydroisoxazolopyridine.Both procedures are illustrated by synthesis of the fire ant-venom alkaloid, solenopsin A.
